These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

255 related items for PubMed ID: 8116671

  • 1. Polydactyly, campomelia, ambiguous genitalia, cystic dysplastic kidneys, and cerebral malformation in a fetus of consanguineous parents: a new multiple malformation syndrome, or a severe form of oral-facial-digital syndrome type IV?
    Adès LC, Clapton WK, Morphett A, Morris LL, Haan EA.
    Am J Med Genet; 1994 Jan 15; 49(2):211-7. PubMed ID: 8116671
    [Abstract] [Full Text] [Related]

  • 2. Oral-facial-digital syndrome type IV (Mohr-Majewski syndrome): a fetopathological study.
    Moerman P, Fryns JP.
    Genet Couns; 1998 Jan 15; 9(1):39-43. PubMed ID: 9555586
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Short rib (polydactyly) syndrome type IV: Beemer-Langer syndrome.
    Sharma AK, Phadke SR, Agarwal SS.
    Am J Med Genet; 1993 May 15; 46(3):345-6. PubMed ID: 8488883
    [No Abstract] [Full Text] [Related]

  • 6. Campomelia, cervical lymphocele, polycystic dysplasia, short gut, polysplenia.
    Cumming WA, Ohlsson A, Ali A.
    Am J Med Genet; 1986 Dec 15; 25(4):783-90. PubMed ID: 3538874
    [Abstract] [Full Text] [Related]

  • 7. Cerebro-reno-digital (Meckel-like) syndrome with Dandy-Walker malformation, cystic kidneys, hepatic fibrosis, and polydactyly.
    Genuardi M, Dionisi-Vici C, Sabetta G, Mignozzi M, Rizzoni G, Cotugno G, Martini Neri ME.
    Am J Med Genet; 1993 Aug 01; 47(1):50-3. PubMed ID: 8368252
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Orofaciodigital syndrome type IV: report of a patient.
    Nevin NC, Thomas PS.
    Am J Med Genet; 1989 Feb 01; 32(2):151-4. PubMed ID: 2929654
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Dandy-Walker malformation (variant), cystic dysplastic kidneys, and hepatic fibrosis: a distinct entity or Meckel syndrome?
    Walpole IR, Goldblatt J, Hockey A, Knowles S.
    Am J Med Genet; 1991 Jun 01; 39(3):294-8. PubMed ID: 1867280
    [Abstract] [Full Text] [Related]

  • 14. Midline malformation syndromes.
    Sharma AK, Phadke SR.
    Am J Med Genet; 1994 Apr 15; 50(3):304-5. PubMed ID: 8042679
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Acrocallosal syndrome in two African brothers born to consanguineous parents.
    Christianson AL, Venter PA, Du Toit JL, Shipalana N, Gericke GS.
    Am J Med Genet; 1994 Jun 01; 51(2):98-101. PubMed ID: 8092201
    [Abstract] [Full Text] [Related]

  • 17. [Mohr's syndrome : type II orofaciodigital syndrome (author's transl)].
    Ajacques JC.
    Rev Stomatol Chir Maxillofac; 1981 Jun 01; 82(4):234-40. PubMed ID: 6269173
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome).
    Koppe R, Kaplan P, Hunter A, MacMurray B.
    Am J Med Genet; 1989 Nov 01; 34(3):305-12. PubMed ID: 2596519
    [Abstract] [Full Text] [Related]

  • 20. Alopecia universalis congenita, XY gonadal dysgenesis and laryngomalacia: a novel malformation syndrome.
    El-Shanti H, Ahmad M, Ajlouni K.
    Eur J Pediatr; 2003 Jan 01; 162(1):36-40. PubMed ID: 12486505
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.